跳至主要内容
临床试验/NCT05216861
NCT05216861招募中不适用

Evaluation of a Collaborative Intervention to Promote Early Employer Contact and Return to Work Among People With Common Mental Disorders or Long-term Pain

Uppsala University2 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2022年2月15日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
120
试验地点
2
主要终点
Sick leave

研究概览

简要总结

The overall aim of this cluster ranomized controlled trial is to investigate whether an intervention for collaboration between patient with CMD or chronic pain and employer (the Demand and Ability Protocol) can contribute to reduced sick leave and to increased health, work ability and trust in the managers. The intervention is delivered by rehabiliation coordinators at primary health care centres.

详细描述

The overall aim of this cluster ranomized controlled trial is to investigate whether an intervention for collaboration between patient with CMD or chronic pain and employer (the Demand and Ability Protocol) can contribute to reduced sick leave and to increased health, work ability and trust in the managers. The intervention is delivered by rehabilitation coordinators at primary health care centres.

Furthermore, the aim is to identify hindering and facilitating factors for feasibility, usability and implementation of the Demand and Ability Protocol intervention (DAP) in primary health care.

Research questions:

  1. What is the effect of DAP for patients regarding sick leave, health, work ability, and trust in the manager compared to matched controls who do not recieve DAP?
  2. How do patients and managers experience their participation in the intervention and how do they experience the usability of the DAP?
  3. What facilitating and hindering factors exist for the introduction and implementation of DAP in primary health care, and how do rehabilitation coordinators (REKO) and medical doctors experience the feasibility and usability of the intervention?

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • have a diagnosis of CMD and/or chronic pain
  • have a job
  • be on full-time or part time sick leave
  • accept the manager's involvement.

排除标准

  • been on full-time sick leave for more than 6 months before the first contact with REKO

结局指标

主要结局

Sick leave

时间窗: From baseline until 12 months

The total number of days on sick leave due to CMDs or chronic pain during the 12 month follow-up period

次要结局

未报告次要终点

研究者

发起方
Uppsala University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Therese Hellman

PhD, Associate professor

Uppsala University

研究点 (2)

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